1,7-肼基转移参与的喹啉脱芳烃化反应生成 C3-螺氢喹啉

Da-Ying Shao, Bin Qiu, Zi-Kang Wang, Zhen-Yuan Liu, Jian Xiao, Xiao-De An
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引用次数: 0

摘要

1,7-氢化物转移参与的喹啉脱芳反应制备了c3 -螺旋型氢喹啉衍生物。该方法提供了一种通过氧化还原-中性氢化物转移过程实现缺电子芳烃脱芳化的方案。具有良好的非对偶选择性,可以得到一系列的c3 -螺环对苯二酚,产率可达98%。高台阶经济性和原子经济性以及氧化还原中性和温和的条件等显著优点使其成为实现喹啉类脱芳化的一种有吸引力的替代方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

1,7-Hydride transfer-involved dearomatization of quinolines to access C3-spiro hydroquinolines

1,7-Hydride transfer-involved dearomatization of quinolines to access C3-spiro hydroquinolines
1,7-Hydride transfer-involved dearomatization of quinolines toward C3-spiro hydroquinoline derivatives has been developed. This method offers a protocol to achieve the dearomatization of electron-deficient arenes via the redox-neutral hydride transfer process. A series of C3-spiro hydroquinolines can be provided in moderate to excellent yields (up to 98 %) with good diastereoselectivities. Significant advantages such as high step- and atom-economy, as well as redox-neutral and mild conditions, make it an appealing alternative to achieve the dearomatization of quinolines.
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